Clinical Trial Manager

Remotedxb; Dubai; On-site; AED 350,000 - 520,000; Full time

Job summary

Iovance Biotherapeutics is seeking an experienced Clinical Trial Manager to oversee execution of multidisciplinary clinical studies from synopsis to final deliverables. You will manage budgets, timelines, and cross-functional teams, ensuring data integrity and on-time progress to senior leadership.

Strong CRO/vendor experience and US/global regulatory expertise are essential. The role requires leadership across phases 1–4, with a focus on oncology programs and rigorous adherence to SOPs,

Qualifications

• Bachelor's degree required.
• 5+ years of pharmaceutical/biotech clinical research or oncology experience.
• At least 1 year of experience as a Clinical Trial Manager (CTM).
• Experience designing and managing Phase 1-4 clinical trials.
• Experience in management and selection of CROs and vendors.
• Subject matter expertise in US and Global Regulations (SOPs, ICH-GCP, FDA-CFR).

Responsibilities

• Support operational execution of clinical studies from synopsis through final project deliverables.
• Manage implementation, budget, milestones, and timelines for clinical studies.
• Oversee cross-functional study teams to ensure execution within budget and timelines.
• Lead vendor identification, qualification, and selection for EDC, IWRS, and Central Laboratories.
• Ensure data integrity through routine reviews, query resolution, and consistency checks.
• Track and communicate program progress to Senior Management via dashboards and trackers.
• Assess the impact of changing regulations and guidance on clinical projects.

Education

Bachelor's degree

Job description

Responsibilities

• Support operational execution of clinical studies from synopsis through final project deliverables
• Manage implementation, budget, milestones, and timelines for clinical studies
• Oversee cross-functional study teams to ensure execution within budget and timelines
• Lead vendor identification, qualification, and selection for EDC, IWRS, and Central Laboratories
• Ensure data integrity through routine reviews, query resolution, and consistency checks
• Track and communicate program progress to Senior Management via dashboards and trackers
• Assess the impact of changing regulations and guidance on clinical projects

Requirements

• Bachelor's degree
• 5+ years of pharmaceutical or biotech-related clinical research or oncology experience
• At least 1 year of experience as a Clinical Trial Manager (CTM)
• Demonstrated experience designing and managing Phase 1-4 clinical trials
• Experience in the management and selection of CROs and vendors
• Subject matter expertise in US and Global Regulations (SOPs, ICH-GCP, FDA-CFR)

About the Company

Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer.